HFE c.109_110delinsTG ;(p.A37C)

Variant ID: 6-26091101-GC-TG

NM_000410.3(HFE):c.109_110delinsTG;(p.A37C)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

A child with hyperferritinemia: case report.

Italian Journal Of Pediatrics
Serra, Melania M; Longo, Filomena F; Roetto, Antonella A; Sandri, Alessandro A; Piga, Antonio A
Publication Date: 2011-05-12

Variant appearance in text: HFE: A37C
PubMed Link: 21569394
Variant Present in the following documents:
  • Main text
  • 1824-7288-37-20.pdf
View BVdb publication page